Verification system for prescription packaging and method

ABSTRACT

A system for verifying medication doses m a filled medication package comprises an imaging unit to produce at least one image of a filled medication package and a verification unit for receiving the image of the filled medication package. The verification unit comprises a dose locator to determine from the image a location of any dose m the filled medication package, and associate a time period to the location. It also comprises a dose verifier to verify an identity of any dose from the visual characteristics of the image as a function of dose reference profiles. The verification unit compares an identity and time period of the doses of the filled medication package to a prescription and has an interface for producing verification output based on the comparison of the verification unit. A method for verifying medication doses m a filled medication package is also provided.

CROSS-REFERENCE TO RELATED APPLICATION

The present application claims priority on U.S. Provisional PatentApplication No. 61/310,896, filed on Mar. 5, 2010, and U.S. ProvisionalPatent Application No. 61/366,649, filed on Jul. 22, 2010, bothincorporated herein by reference.

FIELD OF THE APPLICATION

The present application relates to medication prescription packagingsuch as medication trays and dosage systems filled with medication as afunction of personal prescriptions, and more particularly to theverification of the contents of medication trays and like dosagesystems.

BACKGROUND OF THE ART

Medication trays, blister packs and like dosage systems are useful toolsfor people having to take a variety of medications on a daily basis. Asan example of dosage control packaging, medication trays typicallyconsist of a tray having a plurality of compartments. Each compartmentdefines a period of a day, and is thus filled with the medicationtablets and pills that must be taken at that period. The compartmentsare individually closed with a backing sheet, thereby forming anassembly known as a blister card. The medication trays are commonlydivided into 7 rows of 4 compartments, each row representing a day ofthe week, and each compartment of a row representing a time of day.

Considering that the medication trays are filled with a large quantityof pills and tablets, and considering that improper doses of medicationcan be harmful to individuals, great care is currently taken to ensurethat medication trays are filled in accordance with a prescription. Oneverification step may be done by a pharmacy attendant, who visuallyinspects each compartment and compares the contents to a printedprescription. This is a time-costly process, and even requires in someregions the involvement of the pharmacist, because of regulations.

Similarly, medication packaging (e.g., dosage systems, bulk containers)may contain the incorrect tablets and/or doses, whereby packaging mustoften be verified manually to ensure the precision of the prescription.

SUMMARY OF THE APPLICATION

It is therefore an aim of the present application to provide a novelverification system for medication packaging.

Therefore, in accordance with a first embodiment, there is provided asystem for verifying medication doses in a filled medication package,comprising an imaging unit to produce at least one image of a filledmedication package; a verification unit for receiving the image of thefilled medication package, and comprising: a dose locator to determinefrom the image a location of any dose in the filled medication package,and associate a time period to the location; a dose verifier to verifyan identity of any dose from the visual characteristics of the image asa function of dose reference profiles, whereby the verification unitcompares an identity and time period of the doses of the filledmedication package to a prescription; and an interface for producingverification output based on the comparison of the verification unit.

Further in accordance with the first embodiment, a visualcharacteristics database provides the dose reference profiles to thedose verifier.

Still further in accordance with the first embodiment, the dosereference profiles comprise visual characteristics in the form of atleast one of an outline, a geometry, pattern, color data, marking, codepertaining to a specific dose.

Still further in accordance with the first embodiment, the dosereference profiles also comprise data pertaining to at least one of aname, a reference number, a posology of the specific dose.

Still further in accordance with the first embodiment, the verificationunit comprises a scan reader for at least one of providing dose locationdata to the dose locator, and for identifying a dose.

Still further in accordance with the first embodiment, a patientprescription database for providing prescription profiles is provided,and the dose verifier compares the filled medication package to aprescription profile for an identified patient.

Still further in accordance with the first embodiment, the verificationunit obtains the dose reference profile related to the prescription, andfurther wherein the dose verifier verifies the identity of any dose bycomparing the dose to the obtained dose reference profile.

Still further in accordance with the first embodiment, an image databasefor storing the image for the prescription is provided.

Still further in accordance with the first embodiment, the imaging unitcomprises actuators to displace a camera to produce multiple images ofthe filled medication package.

Still further in accordance with the first embodiment, the imaging unitprovides coordinates of the camera for each of the multiple images, andthe dose locator determines from the coordinates the intake period fordoses in the images.

In accordance with a second embodiment, there is provided a method forverifying medication doses in a filled medication package as a functionof a prescription, comprising: obtaining at least one image of thefilled medication package; determining an intake period of at least onedose from the at least one image; identifying the at least one doseusing visual characteristics of the dose from the image in comparisonwith dose reference profiles; comparing the identity and the intakeperiod of the at least one dose with a prescription; and outputting datarelated to the comparing.

Further in accordance with the second embodiment, obtaining at least oneimage comprises obtaining at least two images and creating at least oneof a three-dimensional image and a mosaic for subsequent steps.

Still further in accordance with the second embodiment, determining theintake period comprises identifying a compartment of the dose in thefilled medication package and associating a day and hour value to thecompartment.

Still further in accordance with the second embodiment, determining theintake period comprises reading location data related to a compartmentof the dose in the filled medication package.

Still further in accordance with the second embodiment, a patientposologic profile related to the prescription is obtained, and comparingcomprises comparing the identity and the intake period of the at leastone dose with the patient posologic profile.

Still further in accordance with the second embodiment, dose referenceprofiles for medication indicated in the patient posologic profile isobtained, and identifying the at least one dose from the image comprisescomparing the visual characteristics of the dose with data of theobtained dose reference profiles.

Still further in accordance with the second embodiment, the at least oneimage with the prescription is stored.

Still further in accordance with the second embodiment, outputting datacomprises indicating to an operator an error requiring additionalverification.

Still further in accordance with the second embodiment, obtaining atleast one image of the filled medication package comprises obtainingcoordinates of a camera producing the image, and determining an intakeperiod comprises determining the intake period using the coordinates.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is block diagram of a verification system for medicationpackaging in accordance with an embodiment of the present application;

FIG. 2 is a block diagram of verification systems of FIG. 1, inconjunction with a pharmacy network; and

FIG. 3 is a flow chart of a method for verifying the contents of amedication packaging in accordance with another embodiment of thepresent disclosure.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring to FIG. 1, a verification system for medication trays isgenerally shown at 10, with respect to a filled medication package A.The medication package A may be any type of package enclosingmedication, such as medication trays, tubular containers, pill packs,blister card or pack, bulk container, PCI controlled dosage system,Pharmacard™, vials, or any other medication packaging. The verificationunit 12 is efficiently used with medication packages of the type havinga plurality of doses of medication, arranged in separate compartments asa function of a patient posologic profile. For simplicity purposes,reference will be made to a medication package A or filled package Ahereafter, but the disclosure is intended to cover uses of theverification system 10 with any appropriate type of medication packages,provided the use is in accordance with the present disclosure. Moreover,reference is made hereafter to the filled package A as comprising pills,with pills referring to any geometrically defined medication doses (asopposed to liquids, powder), such as tablets, capsules, hard gelatincapsules, etc.

The verification system 10 has an imaging unit 11, a verification unit12, and an interface unit 13.

The imaging device 11 obtains images of the filled medication package A.

The verification unit 12 compares the images to data related to aprescription, and performs a verification.

The interface unit 13 outputs a verification report in any appropriateformat, as will be described hereinafter.

The imaging unit 11 is typically a high-resolution digital camera 11A ordigital cameras (e.g., 3CCD camera), that are oriented to take globalimages of the filled package A. In an embodiment, the imaging unit 11comprises a camera 11A positioned above the filled package A to take aplan view of the filled package. As the medication packages such asmedication trays and blister cards may have compartments that arerelatively large, a plan view may be sufficient to show all tablets andpills for subsequent identification. The camera produces an image of thetablets. It may be required to lay all tablets manually to ensure thatat least a full plan view of each tablet may be obtained, or to use atemporary tray to ensure proper images of laid tablets are taken.Alternatively, it may be sufficient to obtain an image of a tabletpartially obstructed by an adjacent tablet. Therefore, the image of thetablet defines at least a partial outline of the tablet, preferably asnaturally lying on a flat surface, but alternatively in any givenorientation, in addition to the color (e.g., tint and contrast). Theimage may also contain ornamentation of the tablet, such as a brandname. The image of the tablet may also comprise an image of a barcode onthe tablet. For instance, some tablets may have on their surface a datamatrix (a.k.a., two-dimensional matrix barcode), which data matrixrepresents full tablet information. Other types of coding may be used aswell.

The imaging unit 11 may comprise more than one camera, for instance toobtain images from different viewpoints. The imaging unit 11 may also bemounted to actuators 11B, to move to different points of view. Forinstance, the imaging unit 11 may be mounted to translation joints, suchas linear actuators, for instance as part of a planar manipulator orrobot. According to an embodiment, at least one image of eachcompartment of the filled package A is obtained, with coordinates of thecamera 11A being tagged with the image by the monitoring of theactuators 11B. It may also be considered to take multiple images of eachsingle compartment, to obtain different focusing and ensure that thedoses will ultimately be identified.

By having multiple images, 2-D mosaics or 3-D images of the pills andtablets may subsequently be produced. The 3-D images are suited forverifying the contents of smaller containers, in which the tablets andpills are randomly packed in height (as opposed to in a plane for thefilled package A), such as in a tubular container. As mentioned above,the digital cameras or equivalent image-producing devices of the imagingunit 11 may also obtain color and tint information from the pills andtablets, for the subsequent identification of the pill/tablet.Accordingly, the imaging unit 11 may comprise its own lighting unit, toensure that suitable lighting is provided to obtain a clear contour ofthe pills/tablets. Moreover, the wavelength of the light produced by theimaging unit 11 may be controlled to ensure that the correct color isreflected back to the digital camera of the imaging unit 11. Thewavelength used by the imaging unit 11 may replicated the wavelengthused to image profile pictures of pills.

The verification unit 12 receives the images of the filled package A orother container from the imaging unit 11, and verifies the contents ofthe package A in comparison with a patient prescription. Theverification unit 12 comprises a verification processor 20 that istypically a processing unit of a computer (PC, laptop, etc) and will runthe verification application. It is considered to use an efficientprocessor (e.g., quad-core processor, among others) to efficientlyperform the verification.

The verification processor 20 accesses a visual characteristics database21, that contains data pertaining to the visual characteristics of thepills and tablets (hereinafter doses). Accordingly, each dose has a dosereference profile, by which each dose is identified in the database 21with a full identification (name, reference number, posologic data),along with an outline, a geometry, a pattern, color data, marking(brand, name, trademark) or a code (e.g., barcode, data matrix, etc).The geometry may consist in a three-dimensional model of the dose, or ina plurality of flat elevation models (e.g., for instance as laid on aflat surface). In the case where the imaging unit 11 has a singlecamera, the dose reference profile may have outline models of the dosefor all possible orientations. The dose reference profile comprisesenough information to differentiate doses from one another.

In an embodiment, medicaments each have a dose reference profile asprovided by the manufacturer of the medicament, as detailed hereafter.Alternatively, the dose reference profiles may be created by theoperator of the verification system 10, or downloaded from an externalsource B. In creating the images of the dose reference profiles and inverifying medication packages with the system 10, similar lighting andbackground conditions may be used.

The verification processor 20 also accesses a patient prescriptiondatabase 22. The prescription database 22 comprises prescription datafor a client/patient. The prescription data is an identification of thedoses that must be taken by the client/patient at specific time periods.The jobs featuring the prescription data may be obtained from a pharmacynetwork B (i.e., LAN, or remote pharmacy server), may be downloaded fromanother source, or may be programmed, stored and updated in theverification system 10. The patient file may be identified by theverification processor 20 using any information obtained from the images(e.g., bar code, data matrix, characters for OCR), or following manualsteps of identification by the operator (e.g., scanning, manual entry ofpatient id). The verification processor 20 may therefore comprise a scanreader to read such codes from the image obtained from the imaging unit11.

When package images are obtained, a dose locator 23 of the verificationunit 12 provides dose location data for each dose identified from thepackage images. More specifically, each detected dose is tagged withlocation data pertaining to the compartment in which the dose isdetected, i.e., day and period of the day. The dose locator 23 mayidentify the location data as a function of the coordinates of thecamera 11A of the imaging unit 11 if an actuator is used to move theimaging unit 11, and/or as a function of the position of images of thedoses on the image sensor of the imaging unit 11 (as matched with a gridpattern related to the type of packages being scanned), and/or as afunction of data manually entered or scanned, among possibilities.Therefore, each imaged dose has coordinates related to location data,and thus related to the posologic profile.

With the package imaged, the dose verifier 24 of the verification unit12 may identify the dose, using the dose reference models from thecharacteristics database 21. Each dose is identified by the name of themedication and posologic data, by comparing the visual attributes(geometry, shape, color, marks, barcode, data matrix) of the doe imagesand the dose reference models of the database 21.

In an embodiment, the dose verifier 24 uses the patient data from thepatient prescription database 22 to obtain the dose reference profiles21 of the doses that are expected per intake period, as per the patientprofile. Accordingly, instead of performing an identification of animage dose among a vast number of images, the dose verifier 24 comparesthe expected dose reference profiles to the dose images. Such acomparison reduces the processing to be performed by the verificationprocessor 20 to verify images, and confirm the identify of the doses.

Therefore, the verification processor 20 combines the doseidentification with the location data for each dose, whereby an actuallist of doses is produced for the filled medication package A beingverified. The actual list of doses is compared with the prescriptiondata for the medication package, namely the desired list of doses perintake time for the medication package. The verification processor 20produces a verification report through the interface unit 13 providingthe comparison data. Accordingly, the verification report may be aconfirmation that the actual list of doses is exact and corresponds tothe patient prescription. The verification report may indicate that somedoses are in excess in given compartments, or alternatively that somedoses are missing from given compartments. The verification report mayalso provide some error messages, requiring a visual inspection by thepharmacy attendant in the event that the package image providesinsufficient visual data for some doses, or that some doses do not matchany dose reference model. Considering the risks related to improperprescription, the verification steps performed by the verificationsystem 10, and the verification report must be precise and accurate, andany potential error must be reported to the pharmacyattendant/pharmacist.

An image database 25 may be used to keep the images of each package Averified by the verification processor 20, with for instance the datarelated to the verification. The files in the image database 25 may beused for subsequent verification.

The interface unit 13 may be a printer, a monitor, data output (e.g., inthe form of a file data for network communication), and/or any othersuitable interface. Accordingly, the interface unit 13 outputs theverification report in any appropriate format, such as a printout, aresult screen, an email, a file, etc.

The verification system 10 may perform other tasks related toidentifying the filled medication package A. For instance, the imagingunit 11 may obtain patient data from the medication package A. Forinstance, the imaging unit 11 may have a bar code reader, and themedication package A may have a bar code representing the patient. Theverification unit 12 may thus automatically obtain the patientprescription from the database 22 if the patient is identified with theimaging unit 11. Also, the verification system 10 may be used toquantify the amount of a same dose in a package, as described brieflyabove when enumerating the various packages A with which theverification system 10 may be used.

Referring to FIG. 2, there is illustrated at 40 a network arrangementfor multiple verification systems 10. In FIG. 2, the verificationsystems 10 are shown as being present in two pharmacies, namely 41A and41B, although numerous other verification systems may be present inother pharmacies in the same network.

Each pharmacy has in addition to the verification system 10 a pharmacycomputer 42, that performs the usual tasks related to prescriptions andpharmacy management: e.g. maintaining and updating patient profiles,managing inventory, etc. The verification system 10 and the pharmacycomputer 42 may be share a single processor or may be two separateunits. If the verification system 10 and the pharmacy computer 42 are asingle processor, the verification unit 12 is part of a softwareperforming the afore-mentioned features.

The pharmacy computers 42 are connected to a pharmacy network 50. Forinstance, the pharmacy network may keep patient prescription profiles,provide medication updates, etc.

The verification systems 10 are connected to a dose reference server 60in a client-server model. The dose reference server 60 is used tomaintain a master of dose reference profiles. Therefore, the dosereference server 60 is operated to store updated visual parameters formedication, for instance in visual format, as well as all relevantinformation related to the medication (e.g. bar codes, data matrix, newformats, new doses). The dose reference server 60 provides updates tothe verification systems 10, in the form of updated or new dosereference profiles, additional or updated information for existingprofiles, etc.

The visual characteristics database 21 of the verification systems 10(FIG. 1) may thus be continuously updated with the profiles from thedose reference server 60. According to another embodiment, theverification systems 10 obtain dose reference profiles on aper-verification basis. For instance, a verification system may downloadspecific dose reference profiles upon identifying the expectedmedication of a patient prescription profile, for subsequentverification. The dose reference server 60 may also or alternativelyprovide the relevant information to or through the pharmacy computer 42.

Referring to FIG. 3, there is illustrated a method for verifyingmedication systems in a medication package. The method 70 may beperformed using the verification system 10 for some steps.

According to 72, at least one image of a filled package is obtained. Theimage is a photography or the like taken by an appropriate camera so asto obtain visual characteristics related to the doses in a filledpackage. The visual characteristics may include any of an outline, ageometry, colors (e.g., tint, contrast), brand, bar code, data matrixand any other appropriate type of identification information.

According to 74, an intake period for the doses of the filled package isidentified, for one or more of the doses. In an embodiment, the filledpackage comprises a plurality of compartments each related to an intakeperiod. The image of step 72 may be used to identify the location of thedose and hence an intake period. To identify the intake period,coordinates related to the image may be interpreted as representing anintake period. The coordinates are related to the position of an imagingunit when taking pictures, with each set of coordinates being associatedwith an intake period. Alternatively, the image may be segmented bycompartment in accordance with a grid representing the filled package,with each box of the grid corresponding to a compartment, and thus to anintake period. Therefore, as each segment of the image is associated toa box of the grid, an intake period is tagged to each of the doses inthe compartment.

It may also be considered to provide data for each compartment (e.g.,bar code, data matrix, characters for OCR), in such a way that theidentification of the intake period for each dose is performed by therecognition of the data from the image of 72.

According to 76, the dose is identified from the image. Theidentification may consist in the comparison of the visualcharacteristics of the doses from the images with dose referenceprofiles from a database.

According to an embodiment, the identification may be the comparison ofthe dose with images of a database of expected doses at the given intakeperiod. In such a case, the identification of the doses is initiated byan identification of the filled package to a patient file, for instanceusing visual data obtained from the image of (e.g., bar code, datamatrix, characters for OCR), or by any other scanning step by anoperator, or by manual data entry by the operator. Once the patient fileis identified, the patient posologic profile may be received along withvisual characteristics of the doses, for the comparison with the imageddoses.

According to 78, the identified dose and the intake period are comparedto the patient posologic profile in order to determine that the filledpackage is correctly filled. The comparison may consist of the creationof a list of identified doses as a function of intake period, adjacentto the same information as obtained from the patient posologic profile.

According to 80, verification data is output to indicate that thepackage is correctly filled or that there may be errors and that furtheridentification is required.

1. A system for verifying medication doses in a filled medicationpackage, comprising an imaging unit to produce at least one image of afilled medication package; a verification unit for receiving the imageof the filled medication package, and comprising: a dose locator todetermine from the image a location of any dose in the filled medicationpackage, and associate a time period to the location; a dose verifier toverify an identity of any dose from the visual characteristics of theimage as a function of dose reference profiles, whereby the verificationunit compares an identity and time period of the doses of the filledmedication package to a prescription; and an interface for producingverification output based on the comparison of the verification unit. 2.The system according to claim 1, further comprising a visualcharacteristics database providing the dose reference profiles to thedose verifier.
 3. The system according to claim 1, wherein the dosereference profiles comprise visual characteristics in the form of atleast one of an outline, a geometry, pattern, color data, marking, codepertaining to a specific dose.
 4. The system according to claim 3,wherein the dose reference profiles further comprise data pertaining toat least one of a name, a reference number, a posology of the specificdose.
 5. The system according to claim 1, wherein the verification unitcomprises a scan reader for at least one of providing dose location datato the dose locator, and for identifying a dose.
 6. The system accordingto claim 1, further comprising a patient prescription database forproviding prescription profiles, and further wherein the dose verifiercompares the filled medication package to a prescription profile for anidentified patient.
 7. The system according to claim 6, wherein theverification unit obtains the dose reference profile related to theprescription, and further wherein the dose verifier verifies theidentity of any dose by comparing the dose to the obtained dosereference profile.
 8. The system according to claim 1, furthercomprising an image database for storing the image for the prescription.9. The system according to claim 1, wherein the imaging unit comprisesactuators to displace a camera to produce multiple images of the filledmedication package.
 10. The system according to claim 9, wherein theimaging unit provides coordinates of the camera for each of the multipleimages, and wherein the dose locator determines from the coordinates theintake period for doses in the images.
 11. A method for verifyingmedication doses in a filled medication package as a function of aprescription, comprising: obtaining at least one image of the filledmedication package; determining an intake period of at least one dosefrom the at least one image; identifying the at least one dose usingvisual characteristics of the dose from the image in comparison withdose reference profiles; comparing the identity and the intake period ofthe at least one dose with a prescription; and outputting data relatedto the comparing.
 12. The method according to claim 11, whereinobtaining at least one image comprises obtaining at least two images andcreating at least one of a three-dimensional image and a mosaic forsubsequent steps.
 13. The method according to claim 11, whereindetermining the intake period comprises identifying a compartment of thedose in the filled medication package and associating a day and hourvalue to the compartment.
 14. The method according to claim 11, whereindetermining the intake period comprises reading location data related toa compartment of the dose in the filled medication package.
 15. Themethod according to claim 11, further comprising obtaining a patientposologic profile related to the prescription, and wherein comparingcomprises comparing the identity and the intake period of the at leastone dose with the patient posologic profile.
 16. The method according toclaim 15, further comprising obtaining dose reference profiles formedication indicated in the patient posologic profile, and whereinidentifying the at least one dose from the image comprises comparing thevisual characteristics of the dose with data of the obtained dosereference profiles.
 17. The method according to claim 11, furthercomprising storing the at least one image with the prescription.
 18. Themethod according to claim 11, wherein outputting data comprisesindicating to an operator an error requiring additional verification.19. The method according to claim 11, wherein obtaining at least oneimage of the filled medication package comprises obtaining coordinatesof a camera producing the image, and wherein determining an intakeperiod comprises determining the intake period using the coordinates.